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FDA 510(k)

STORZ, ALPHA II BIOMETRIC RULER

K-Number: K860553 · 1986-06-16

ApplicantStorz Instrument Co.
Decision Date1986-06-16
Product CodeITX
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

STORZ, ALPHA II BIOMETRIC RULER is the device name listed in this FDA 510(k) record. The listed applicant is Storz Instrument Co.. It received FDA 510(k) clearance on 1986-06-16 under 510(k) number K860553. The device is classified under product code ITX. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STORZ, ALPHA II BIOMETRIC RULER?

STORZ, ALPHA II BIOMETRIC RULER is a medical device that received FDA 510(k) clearance on 1986-06-16. The listed applicant is Storz Instrument Co.. The 510(k) number is K860553.

When did STORZ, ALPHA II BIOMETRIC RULER receive FDA 510(k) clearance?

STORZ, ALPHA II BIOMETRIC RULER received FDA 510(k) clearance on 1986-06-16, under 510(k) number K860553.

Who is the listed applicant for STORZ, ALPHA II BIOMETRIC RULER?

The FDA 510(k) record lists Storz Instrument Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STORZ, ALPHA II BIOMETRIC RULER?

The FDA product code for STORZ, ALPHA II BIOMETRIC RULER is ITX.

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Other records listing Storz Instrument Co. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K980100STORZ DP4210 VENTURI ECONOMY ANTERIOR PACK AND DP5000 ASC DAYPACKK980488STORZ MILLENNIUM MICROSURGICL SYSTEM HIGH SPEED VITRECTOMY SYSTEMK972664STORZ MILLENNIUM VISCOUS FLUID SYSTEMK971439STORZ MICROFLOW AND STORZ STANDARD PHACOEMULSIFICATION NEEDLESK964743STORZ E8010 ERGOTEC/PREMIERE ADAPTORK960024STORZ D7120 PHACO HANDPIECE MAINTENANCE KIT & STORZ D7125 PHACO HANDPIECE NEEDLE WRENCH

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Related Devices (Code: ITX)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K260114Align® Cover and Pad Guidance ToolCIVCO Medical Instruments Co., Inc.K261170BA-004CCFujifilm CorporationK254143EM-TECH Passive Ultrasound Probe StrapEM-TECH Solutions, Inc.K260161SmartGuide Disposable Guides and GridsUC-CARE , Ltd.K262474ND Needle Guidance SystemAccurate Access, LLCK261014Accuro® 3S Needle Guide KitRivanna Medical, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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